Canonical Allele Identifier: CA2336421213

Gene: TGFB1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41342383_41342387delinsGCTCT , CM000681.2:g.41342383_41342387delinsGCTCT	GRCh38
NC_000019.9:g.41848288_41848292delinsGCTCT , CM000681.1:g.41848288_41848292delinsGCTCT	GRCh37
NC_000019.8:g.46540128_46540132delinsGCTCT	NCBI36
NG_013364.1:g.16540_16544delinsAGAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.635-140_635-136delinsAGAGC MANE Select	ENSP00000221930.4:n.635-140_635-136delinsAGAGC
ENST00000600196.2:c.635-140_635-136delinsAGAGC	ENSP00000504008.1:n.635-140_635-136delinsAGAGC
ENST00000677934.1:c.634+2360_634+2364delinsAGAGC	ENSP00000504769.1:n.634+2360_634+2364delinsAGAGC
ENST00000221930.5:c.635-140_635-136delinsAGAGC	ENSP00000221930.4:n.635-140_635-136delinsAGAGC
ENST00000597453.1:n.166-140_166-136delinsAGAGC
ENST00000600196.1:n.95-140_95-136delinsAGAGC
NM_000660.5:c.635-140_635-136delinsAGAGC	NP_000651.3:n.635-140_635-136delinsAGAGC
XM_011527242.1:c.635-140_635-136delinsAGAGC	XP_011525544.1:n.635-140_635-136delinsAGAGC
NM_000660.6:c.635-140_635-136delinsAGAGC	NP_000651.3:n.635-140_635-136delinsAGAGC
XM_011527242.2:c.635-140_635-136delinsAGAGC	XP_011525544.1:n.635-140_635-136delinsAGAGC
NM_000660.7:c.635-140_635-136delinsAGAGC MANE Select	NP_000651.3:n.635-140_635-136delinsAGAGC